马凡氏综合征与妊娠:临床意义和处理

Fetal and maternal medicine review Pub Date : 2010-08-01 DOI:10.1017/S0965539510000082

Ariadna Grigoriu, J. Colman, C. Silversides, R. Wald, S. Siu, M. Sermer

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引用次数: 0

摘要

马凡氏综合征(MFS)是一种常染色体显性结缔组织疾病，影响多器官系统，主要是心血管、眼和骨骼。这是影响心脏和主动脉的最常见的遗传性疾病，发病率为1:5000-1:9800。没有种族或性别倾向;20%至35%的病例是由新生突变引起的。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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MARFAN SYNDROME AND PREGNANCY: CLINICAL IMPLICATIONS AND MANAGEMENT

Marfan syndrome (MFS) is an autosomal dominant connective tissue disorder that affects multiple organ systems, primarily the cardiovascular, ocular and skeletal. It is the most common inherited condition affecting the heart and the aorta, occurring in 1:5000–1:9800 people. There is no ethnic or gender predisposition; 20 to 35% of cases arise from de novo mutations.

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Fetal and maternal medicine review

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